Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Tamara Ilisic"'
Autor:
Gordana Milosevski-Lomic, Amira Peco-Antic, Aleksandra Vukašinović, Tamara Ilisic, Jelena Kotur-Stevuljevic, Dusan Paripovic
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation
Oxidative stress seems to be an important link between obesity and cardiovascular disease. The aim of our study was to assess oxidative stress in obese patients stratified according to ambulatory blood pressure status and to determine independent pre
Publikováno v:
Cardiology. 134:375-380
A double-chambered right ventricle (DCRV) is an uncommon congenital anomaly: the right ventricle (RV) is divided into two chambers due to the presence of an abnormally located muscular band or anomalous muscle hypertrophy in the subinfundibular part
Autor:
Igor Stefanovic, Irena Vulicevic, Vladimir Milovanovic, Vojislav Parezanovic, Goran Vukomanovic, Tamara Ilisic, Branko Mimic, Jasna Kalanj, Ida Jovanovic, Milan Djukic, Slobodan Ilic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 143, Iss 9-10, Pp 559-566 (2015)
Introduction. Diagnosis of neonatal coarctation of the aorta (CoA) still presents a challenge in routine practice because of absence of reliable morphologic and functional parameters for early detection of this congenital heart defect in newborns. Ob
Autor:
Vojislav Parezanovic, Ida Jovanovic, Ivan Divac, Tamara Ilisic, Milan Djukic, Irena Vulicevic, Branko Mimic, Vladimir Milovanovic, Slobodan Ilic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 142, Iss 3-4, Pp 164-169 (2014)
Introduction. Total anomalous pulmonary venous connection (TAPVC) is a rare congenital heart disease and in some variants represents the only true surgical emergency in congenital heart surgery. Basic anatomical characteristic of this anomaly is an a
Autor:
Goran Vukomanovic, Irena Vulicevic, Tamara Ilisic, Slobodan Ilic, Vojislav Parezanovic, Sanja Dzelebdzic, Ida Jovanovic, Milan Djukic, Igor Stefanovic, Jasna Kalanj
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 142, Iss 9-10, Pp 542-546 (2014)
Introduction. Pulmonary artery stenosis (PS) is a congenital heart defect which occurs in 10% of all congenital heart defects. Pulmonary balloon valvuloplasty (BVP) has been the treatment of choice of PS over the last 30 years. Objective. The purpose
Autor:
Irena Vulicevic, Ida Jovanovic, Milan Djukic, Vojislav Parezanovic, Marija Gradinac, Igor Stefanovic, Tamara Ilisic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 141, Iss 11-12, Pp 803-806 (2013)
Introduction. Critical congenital heart diseases (CHD) are mostly duct-dependent and require stable systemic-pulmonary communication. In order to maintain patency of the ductus arteriosus (DA), the first line treatment is Prostaglandin E1 and the sec
Autor:
Slobodan Ilic, Djordje Hercog, Milincić Z, Vulićevuć I, Goran Vukomanovic, Branko Mimic, Parezanović, Slavko Simeunovic, Milan Vucicevic, Tamara Ilisic, Brajković Z, Ida Jovanovic, Milan Djukic
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 132:9-13
Cyanotic heart diseases are relatively rare, but they are severe and heterogeneous congenital heart diseases, which require complex surgery. Development of different advanced surgical procedures, such as arterial switch operation (ASO), Fontan and it
Autor:
Ida Jovanovic, Vojislav Parezanovic, Tamara Ilisic, Ingo Daehnert, Irena Vulicevic, Jasna Kalanj, Milan Djukic, Ana Gligic, Slobodan Ilic, Igor Stefanovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 142, Iss 1-2, Pp 17-22 (2014)
Introduction. Balloon valvuloplasty (BVP) is one of the primary therapies for congenital aortic stenosis in children and adolescents. The aim of this interventional procedure is to gain time before possible surgical therapy (aortic valve replacement)
Autor:
Ida Jovanovic, Milan Djukic, Slobodan Ilic, Djordje Hercog, Tamara Ilisic, Irena Vulicevic, Milan Vucicevic, Branko Mimic, Vojislav Parezanovic
Publikováno v:
The Annals of thoracic surgery. 97(2)
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) represents one of the most common causes of myocardial ischemia in infants and if left untreated results in a high mortality rate. When ALCAPA coexists with other congeni
Autor:
Tamara Ilisic, Marija Gradinac, Milena Milivojevic, Ida Jovanovic, Danijela Drakulic, Milena Stevanovic, Aleksandar Krstic, Goran Cuturilo, Vojislav Parezanovic
Publikováno v:
Cardiology in the young. 23(2)
Malposition of the branch pulmonary arteries is a rare malformation with two forms. In the typical form, pulmonary arteries cross each other as they proceed to their respective lungs. The “lesser form” is characterised by the left pulmonary arter